immunodeficiency 132b
MONDO:0976228Mondo
Findings
No curated finding names immunodeficiency 132b yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Juvenile onset · Childhood onset
HPO, annotations 2026-09-02
Features
50 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormal pulmonary interstitial morphologyHPOHP:0006530
- 1 of 1 reported patient
- ArthritisHPOHP:0001369
- 1 of 1 reported patient
- Atopic dermatitisHPOHP:0001047
- 3 of 3 reported patients
- Atrophic gastritisHPOHP:0002582
- 1 of 1 reported patient
- Celiac diseaseHPOHP:0002608
- 1 of 1 reported patient
- Cervical lymphadenopathyHPOHP:0025289
- 1 of 1 reported patient
- Chronic diarrheaHPOHP:0002028
- 1 of 1 reported patient
- Decreased circulating immunoglobulin concentrationHPOHP:0004313
- 2 of 2 reported patients
- Decreased specific antibody response to protein vaccineHPOHP:0410294
- 1 of 1 reported patient
- Decreased specific antibody response to unconjugated polysaccharide vaccineHPOHP:0410299
- 6 of 6 reported patients
- Decreased total lymphocyte countHPOHP:0001888
- 1 of 1 reported patient
- Drug allergyHPOHP:0410323
- 1 of 1 reported patient
Show the remaining 38
- Enlarged tonsilsHPOHP:0030812
- 1 of 1 reported patient
- HepatomegalyHPOHP:0002240
- 1 of 1 reported patient
- IleitisHPOHP:0032564
- 2 of 2 reported patients
- Increased size of nasopharyngeal adenoidsHPOHP:0040261
- 1 of 1 reported patient
- Inguinal lymphadenopathyHPOHP:0034751
- 1 of 1 reported patient
- LymphadenopathyHPOHP:0002716
- 2 of 2 reported patients
Where it sits
- A kind of